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Class III: unlikely to cause harmTerminated

GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline Nicorette Lozenge Recall

Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination

GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline · Aiken, SC

Risk level
Class III
Reported by FDA
Apr 30, 2014
Recall ID
D-1244-2014
Check your lot numberHow we source this data

Summary

GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline recalled Nicorette Lozenge starting Feb 20, 2014. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1244-2014 on Apr 30, 2014. Reason: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent. Status: Terminated.

Why it was recalled

Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.

Product description

Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination. Contains 30 Pieces/ Pallet. OTC only. GlaxoSmithKlein, 1000 GSK Drive, Moon Township, PA 15108. UPC: 0-03-0766-1442-81-2.

Lot numbers, UPCs & expiration codes

Lot #12K16W (exp 5/14), 12K27N (exp 6/14), 12K27W (exp 6/14), 12K29N (exp 6/14), 13K20W (exp 6/15), 13K20W1 (exp 6/15) & 13K25N (exp 6/15).

Where it was sold

U.S. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1244-2014
Classification
Class III
Status
Terminated
Recall initiated
Feb 20, 2014
FDA report date
Apr 30, 2014
Quantity
12,162 Pallets
Recall type
Voluntary: Firm initiated
Recalling firm
GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Original FDA data

Every field from FDA enforcement report D-1244-2014, exactly as published.

Show all FDA fields
City
Aiken
State
SC
Status
Terminated
Country
United States
Event ID
67800
Address
65 Windham Blvd
Code information
Lot #12K16W (exp 5/14), 12K27N (exp 6/14), 12K27W (exp 6/14), 12K29N (exp 6/14), 13K20W (exp 6/15), 13K20W1 (exp 6/15) & 13K25N (exp 6/15).
Postal code
29805-9384
Report date
Apr 30, 2014
Product type
Drugs
Recall number
D-1244-2014
Classification
Class III
Recalling firm
GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline
Product quantity
12,162 Pallets
Termination date
Jan 20, 2017
Reason for recall
Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and sub and superpotent.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination. Contains 30 Pieces/ Pallet. OTC only. GlaxoSmithKlein, 1000 GSK Drive, Moon Township, PA 15108. UPC: 0-03-0766-1442-81-2.
Distribution pattern
U.S. Nationwide
Recall initiation date
Feb 20, 2014
Initial firm notification
Letter
Center classification date
Apr 18, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1244-2014, published Apr 30, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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